DE1264750B - Verwendung bestimmter Trioxanmischpolymerisate zum Extrudieren bzw. Tiefziehen - Google Patents
Verwendung bestimmter Trioxanmischpolymerisate zum Extrudieren bzw. TiefziehenInfo
- Publication number
- DE1264750B DE1264750B DEF47082A DEF0047082A DE1264750B DE 1264750 B DE1264750 B DE 1264750B DE F47082 A DEF47082 A DE F47082A DE F0047082 A DEF0047082 A DE F0047082A DE 1264750 B DE1264750 B DE 1264750B
- Authority
- DE
- Germany
- Prior art keywords
- radical
- trioxane
- extrusion
- cyclic
- deep drawing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920001577 copolymer Polymers 0.000 title claims description 10
- 238000001125 extrusion Methods 0.000 title claims description 7
- -1 alkyl radical Chemical class 0.000 claims description 52
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 150000005840 aryl radicals Chemical class 0.000 claims description 7
- 230000001588 bifunctional effect Effects 0.000 claims description 7
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- 239000011888 foil Substances 0.000 claims 1
- 229920006324 polyoxymethylene Polymers 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 239000000155 melt Substances 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000001273 butane Substances 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 229930040373 Paraformaldehyde Natural products 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 150000004292 cyclic ethers Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 238000006798 ring closing metathesis reaction Methods 0.000 description 2
- 238000003856 thermoforming Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- AUAGGMPIKOZAJZ-UHFFFAOYSA-N 1,3,6-trioxocane Chemical compound C1COCOCCO1 AUAGGMPIKOZAJZ-UHFFFAOYSA-N 0.000 description 1
- ZARFQNCGCXIJKV-UHFFFAOYSA-N 1,3-bis(methylsulfonyl)imidazolidine Chemical compound CS(=O)(=O)N1CCN(S(C)(=O)=O)C1 ZARFQNCGCXIJKV-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- WJJSZTJGFCFNKI-UHFFFAOYSA-N 1,3-oxathiolane Chemical compound C1CSCO1 WJJSZTJGFCFNKI-UHFFFAOYSA-N 0.000 description 1
- WUIJTQZXUURFQU-UHFFFAOYSA-N 1-methylsulfonylethene Chemical class CS(=O)(=O)C=C WUIJTQZXUURFQU-UHFFFAOYSA-N 0.000 description 1
- MBNVSWHUJDDZRH-UHFFFAOYSA-N 2-methylthiirane Chemical compound CC1CS1 MBNVSWHUJDDZRH-UHFFFAOYSA-N 0.000 description 1
- SFXNZFATUMWBHR-UHFFFAOYSA-N 2-morpholin-4-yl-2-pyridin-3-ylacetonitrile Chemical compound C=1C=CN=CC=1C(C#N)N1CCOCC1 SFXNZFATUMWBHR-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical class C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- VCZKTIKPEDMZNW-UHFFFAOYSA-N O=S(=O)=S Chemical group O=S(=O)=S VCZKTIKPEDMZNW-UHFFFAOYSA-N 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- VZHRPLJULARYDO-UHFFFAOYSA-N butane-1,4-disulfonyl chloride Chemical compound ClS(=O)(=O)CCCCS(Cl)(=O)=O VZHRPLJULARYDO-UHFFFAOYSA-N 0.000 description 1
- 229930188620 butyrolactone Natural products 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 150000004294 cyclic thioethers Chemical class 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010096 film blowing Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- KOTXCAOSNRHIMI-UHFFFAOYSA-N n-(2-aminoethyl)-1-phenylmethanesulfonamide Chemical compound NCCNS(=O)(=O)CC1=CC=CC=C1 KOTXCAOSNRHIMI-UHFFFAOYSA-N 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 229950006389 thiodiglycol Drugs 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2/00—Addition polymers of aldehydes or cyclic oligomers thereof or of ketones; Addition copolymers thereof with less than 50 molar percent of other substances
- C08G2/18—Copolymerisation of aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/04—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19651570601 DE1570601A1 (de) | 1965-09-03 | 1965-09-03 | Verfahren zur Herstellung von stickstoffhaltigen Copolymeren des Formaldehyds |
| DEF47082A DE1264750B (de) | 1965-09-03 | 1965-09-03 | Verwendung bestimmter Trioxanmischpolymerisate zum Extrudieren bzw. Tiefziehen |
| IL26252A IL26252A (en) | 1965-09-03 | 1966-08-02 | Thermoplastic moulding composition |
| US570438A US3527733A (en) | 1965-09-03 | 1966-08-05 | Copolymers of formaldehyde containing bis - (n' - toluosulphonyl - imidazolidinyl-n-sulphonyl)-alkane |
| SE11628/66A SE349820B (enrdf_load_stackoverflow) | 1965-09-03 | 1966-08-29 | |
| NL6612288A NL6612288A (enrdf_load_stackoverflow) | 1965-09-03 | 1966-08-31 | |
| CH1273966A CH484961A (de) | 1965-09-03 | 1966-09-02 | Verfahren zur Herstellung von stickstoffhaltigen Copolymeren des Formaldehyds |
| BE686377D BE686377A (enrdf_load_stackoverflow) | 1965-09-03 | 1966-09-02 | |
| GB39401/66A GB1154616A (en) | 1965-09-03 | 1966-09-02 | Thermostable Copolymers of Trioxane |
| FR75119A FR1513301A (fr) | 1965-09-03 | 1966-09-02 | Procédé de préparation de copolymères azotés du formaldéhyde |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0047083 | 1965-09-03 | ||
| DEF47082A DE1264750B (de) | 1965-09-03 | 1965-09-03 | Verwendung bestimmter Trioxanmischpolymerisate zum Extrudieren bzw. Tiefziehen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1264750B true DE1264750B (de) | 1968-03-28 |
Family
ID=25976958
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF47082A Pending DE1264750B (de) | 1965-09-03 | 1965-09-03 | Verwendung bestimmter Trioxanmischpolymerisate zum Extrudieren bzw. Tiefziehen |
| DE19651570601 Pending DE1570601A1 (de) | 1965-09-03 | 1965-09-03 | Verfahren zur Herstellung von stickstoffhaltigen Copolymeren des Formaldehyds |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19651570601 Pending DE1570601A1 (de) | 1965-09-03 | 1965-09-03 | Verfahren zur Herstellung von stickstoffhaltigen Copolymeren des Formaldehyds |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3527733A (enrdf_load_stackoverflow) |
| BE (1) | BE686377A (enrdf_load_stackoverflow) |
| CH (1) | CH484961A (enrdf_load_stackoverflow) |
| DE (2) | DE1264750B (enrdf_load_stackoverflow) |
| FR (1) | FR1513301A (enrdf_load_stackoverflow) |
| GB (1) | GB1154616A (enrdf_load_stackoverflow) |
| IL (1) | IL26252A (enrdf_load_stackoverflow) |
| NL (1) | NL6612288A (enrdf_load_stackoverflow) |
| SE (1) | SE349820B (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2430772A1 (de) * | 1973-06-28 | 1975-01-23 | Nat Research Dev Corp London | Verfahren zur herstellung orientierter polymerisatmaterialien |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10214161C1 (de) * | 2002-03-28 | 2003-05-28 | Willibald Hergeth | Behältnis und Palette zur Aufnahme von Schaufeln einer Strömungsmaschine |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1218154B (de) * | 1964-04-20 | 1966-06-02 | Bayer Ag | Verfahren zur Herstellung von Copolymerisaten des Trioxans |
-
1965
- 1965-09-03 DE DEF47082A patent/DE1264750B/de active Pending
- 1965-09-03 DE DE19651570601 patent/DE1570601A1/de active Pending
-
1966
- 1966-08-02 IL IL26252A patent/IL26252A/en unknown
- 1966-08-05 US US570438A patent/US3527733A/en not_active Expired - Lifetime
- 1966-08-29 SE SE11628/66A patent/SE349820B/xx unknown
- 1966-08-31 NL NL6612288A patent/NL6612288A/xx unknown
- 1966-09-02 GB GB39401/66A patent/GB1154616A/en not_active Expired
- 1966-09-02 CH CH1273966A patent/CH484961A/de not_active IP Right Cessation
- 1966-09-02 BE BE686377D patent/BE686377A/xx unknown
- 1966-09-02 FR FR75119A patent/FR1513301A/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2430772A1 (de) * | 1973-06-28 | 1975-01-23 | Nat Research Dev Corp London | Verfahren zur herstellung orientierter polymerisatmaterialien |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1570601A1 (de) | 1970-02-05 |
| GB1154616A (en) | 1969-06-11 |
| US3527733A (en) | 1970-09-08 |
| FR1513301A (fr) | 1968-02-16 |
| NL6612288A (enrdf_load_stackoverflow) | 1967-03-06 |
| SE349820B (enrdf_load_stackoverflow) | 1972-10-09 |
| BE686377A (enrdf_load_stackoverflow) | 1967-02-15 |
| IL26252A (en) | 1971-01-28 |
| CH484961A (de) | 1970-01-31 |
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